Abstract
Two new saponins, 3-O-$(6-O-sulfonyl-β-D-glucopyranosyl-(1→3) $)-α-L-arabinopyranosyl pseudojujubogenin (1) and 3-O-$(α-L-arabinofuranosyl-(1→2)$)- α-L-arabinopyranosyl jujubogenin (2), a new matsutaka alcohol derivative, (3R)-1-octan-3-yl-(6-O-sulfonyl)-β-D-glucopyranoside (3), a new phenylethanoid glycoside, 3,4-dihydroxyphenylethyl alcohol (2-O-feruloyl)-β-D-glucopyranoside (4), and a new glycoside, phenylethyl alcohol $(5-O-p-hydroxybenzoyl-β-D-apiofuranosyl-(1→2) $)-β-D-glucopyranoside (5), were isolated from Bacopa monniera. Their structures were established by NMR, MS, and chemical methods.
Original language | English |
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Pages (from-to) | 1759-1763 |
Number of pages | 5 |
Journal | Journal of Natural Products |
Volume | 65 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 1 2002 |
ASJC Scopus subject areas
- Drug Discovery
- Analytical Chemistry
- Molecular Medicine
- Complementary and alternative medicine
- Pharmacology
- Pharmaceutical Science
- Organic Chemistry